Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
75 participants
INTERVENTIONAL
2024-08-15
2024-09-30
Brief Summary
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This study was planned to recruit 75 patients diagnosed with schizophrenia from the hospital.
A single online tDCS (2 mA × 20 min) and tACS (1.5 mA × 20 min, theta rhythm) intervention was conducted during which participants performed a temporal-sequence memory task for visual pictures, and test scores were compared for each stimulus type on an intermediate test and repetition of the two strategies of learning.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Anodal group
In the anodal group, the anode was placed over the left DLPFC (F3), and the cathode was placed over the contralateral supraorbital area (FP2). A direct current of 2mA was applied for 20 minutes during each stimulation session.
Transcranial direct current stimulation (tDCS)- anodal group
2mA/20mins/session;
Sham group
In the sham group, the stimulation parameters, including the stimulation site and duration, were identical to those of the anodal group. However, during the 10-second ramp-up and ramp-down periods before and after stimulation, patients were unaware that the current was turned off.
Transcranial direct current stimulation (tDCS)- sham group
0mA/20mins/session
tACS group
In the transcranial alternating current stimulation (tACS) group, the anode was placed in the left DLPFC (F3) and the cathode was placed in the contralateral supraorbital region (FP2). A direct current of 1.5 mA was applied for 20 minutes during each stimulation, theta rhythm, 6 HZ.
transcranial alternating current stimulation (tACS)-tACS group
1.5 mA/20 min/session; 6HZ, theta
Interventions
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Transcranial direct current stimulation (tDCS)- anodal group
2mA/20mins/session;
Transcranial direct current stimulation (tDCS)- sham group
0mA/20mins/session
transcranial alternating current stimulation (tACS)-tACS group
1.5 mA/20 min/session; 6HZ, theta
Eligibility Criteria
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Inclusion Criteria
2. Aged 18 years or older, regardless of gender, with an educational level of elementary school or above;
3. All patients received stable-level antipsychotic medication treatment, were in a stable phase of disease treatment, able to understand the testing requirements, and cooperated to complete all research tasks;
4. No history of neurological disorders or other serious physical illnesses, and no history of intellectual disability;
5. No color blindness, color weakness, or other color vision impairments, with normal vision or corrected vision.
Exclusion Criteria
2. Individuals with mental disorders caused by substance dependence or abuse, or the use of psychoactive substances;
3. History of brain injury or other central nervous system-related organic diseases;
4. Individuals at significant risk of suicide or harming others;
5. Participation in similar experiments in the past 30 days prior to baseline.
18 Years
50 Years
ALL
No
Sponsors
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Xiaofeng Ma
OTHER
Responsible Party
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Xiaofeng Ma
Professor
Principal Investigators
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Xiaofeng Ma, Professor
Role: PRINCIPAL_INVESTIGATOR
Northwest Normal University
Locations
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Northwest Normal University
Lanzhou, Gansu, China
Countries
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Central Contacts
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Facility Contacts
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Xiaofeng Ma, Professor
Role: primary
Provided Documents
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Document Type: Study Protocol
Document Type: Informed Consent Form
Other Identifiers
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No.2024018
Identifier Type: -
Identifier Source: org_study_id
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